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1539-04-4

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1539-04-4 Usage

Uses

Diphenyl Terephthalate is used in the preparation of block copolymers, in the preparation of various marerials requiring differing textures.

Check Digit Verification of cas no

The CAS Registry Mumber 1539-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1539-04:
(6*1)+(5*5)+(4*3)+(3*9)+(2*0)+(1*4)=74
74 % 10 = 4
So 1539-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H14O4/c21-19(23-17-7-3-1-4-8-17)15-11-13-16(14-12-15)20(22)24-18-9-5-2-6-10-18/h1-14H

1539-04-4 Well-known Company Product Price

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  • Alfa Aesar

  • (L02877)  Diphenyl terephthalate, 97%   

  • 1539-04-4

  • 5g

  • 778.0CNY

  • Detail
  • Alfa Aesar

  • (L02877)  Diphenyl terephthalate, 97%   

  • 1539-04-4

  • 25g

  • 2778.0CNY

  • Detail

1539-04-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Diphenyl Terephthalate

1.2 Other means of identification

Product number -
Other names diphenyl benzene-1,4-dicarboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1539-04-4 SDS

1539-04-4Relevant articles and documents

Fourier transform Raman spectroscopic study of main-chain thermotropic liquid crystalline polyesters

Ellis, G.,Lorente, J.,Marco, C.,Gomez, M. A.,Fatou, J. G.,Hendra, P. J.

, p. 1353 - 1366 (1991)

The Fourier transform infrared and Raman spectra of the semi-flexible main-chain thermotropic liquid crystal polyester, poly(heptamethylene terephthaloyl-bis-4-oxybenzoate) are presented, and tentative band assignments given.The polymer is investigated as a function of its thermal history, and Fourier transform Raman spectra are recorded with temperature using a high-temperature cell.The results are discussed along with calorimetric and X-ray scattering data.Spectral evidence is presented which is related to both the sample crystallinity, and the crystal-to-liquid crystal phase transition.

1. 4 - b (4 - hydroxybenzene acyl) rectifying section polyetherketoneetherketoneketone copolymer preparation method

-

Paragraph 0022-0023, (2017/08/25)

The invention relates to a 1,4-dis(4-hydroxyl pyrazolyl)benzene and a preparation method of a polyetheretherketone copolymer, which belongs to the high-molecular material field. The method comprises the following steps: selecting nitrobenzene and tetrachloroethanes as solvents, taking aluminium trichloride as a catalyst for a Fries rearrangement reaction to obtain a 1,4-dis(4-hydroxyl pyrazolyl)benzene monomer, then adding 4,4'-difluorobenzophenone and sulfobenzide in a reaction container equipped with a thermometer, protecting under nitrogen, heating to 160-180 DEG C and adding carbonate, heating to 165-190 DEG C and adding a bisphenol monomer, wherein the bisphenol monomer is a mixture of hydroquinone and 1,4-dis(4-hydroxyl pyrazolyl)benzene, performing a program temperature control reaction to obtain a polymer, and processing to obtain the refined polyetheretherketone random polymer.

Molybdenum hexacarbonyl mediated alkoxycarbonylation of aryl halides

Ren, Wei,Emi,Yamane, Motoki

experimental part, p. 2303 - 2309 (2011/09/19)

Mo(CO)mediates the alkoxycarbonylation of aryl halides in their reaction with alcohols to afford arenecarboxylic acid esters. The molybdenum carbonyl complexes act as the catalyst and the source with carbon monoxide. The alkoxycarbonylation proceeds with a small excess of carbon monoxide in the form of Mo(CO)and the procedure is simple compared to the conventional method, which uses palladium catalyst under gaseous carbon monoxide. Using this procedure, a variety of carboxylic acid esters were prepared. Georg Thieme Verlag Stuttgart ? New York.

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